Reckitt Benckiser LLC recalls Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (ND
Recalled April 29, 2015 · FDA recall D-0964-2015 · Reckitt Benckiser
Hazard
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch · FDA Class III
Units
155 cases (2000 pouches of 2 tablets per case)
Sold at
Nationwide
Description
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
Product
Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-0224 Made in England
Manufacturer(s)
Reckitt Benckiser LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →